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α-Acyl lactams in the synthesis of physiologically active compounds

Valentin Georgievich Nenajdenko 1
Valentin Georgievich Nenajdenko
, 
Eugene Pavlovich Zakurdaev 1
Eugene Pavlovich Zakurdaev
, 
Elizabeth Sergeevna Balenkova 1
Elizabeth Sergeevna Balenkova
1 Lomonosov Moscow State University, Faculty of Chemistry
10.1070/RC2009v078n05ABEH004045
Published 30 November 2008
Communication , Volume 78, Issue 5, 431-456
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Nenajdenko V. G., Zakurdaev E. P., Balenkova E. S. α-Acyl lactams in the synthesis of physiologically active compounds // Russian Chemical Reviews. 2009. Vol. 78. No. 5. pp. 431-456.
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Nenajdenko V. G., Zakurdaev E. P., Balenkova E. S. α-Acyl lactams in the synthesis of physiologically active compounds // Russian Chemical Reviews. 2009. Vol. 78. No. 5. pp. 431-456.
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TY - JOUR
DO - 10.1070/RC2009v078n05ABEH004045
UR - https://rcr.colab.ws/publications/10.1070/RC2009v078n05ABEH004045
TI - α-Acyl lactams in the synthesis of physiologically active compounds
T2 - Russian Chemical Reviews
AU - Nenajdenko, Valentin Georgievich
AU - Zakurdaev, Eugene Pavlovich
AU - Balenkova, Elizabeth Sergeevna
PY - 2009
DA - 2008/11/30
PB - ANO Editorial Board of the journal Uspekhi Khimii
SP - 431-456
IS - 5
VL - 78
ER -
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@article{2009_Nenajdenko,
author = {Valentin Georgievich Nenajdenko and Eugene Pavlovich Zakurdaev and Elizabeth Sergeevna Balenkova},
title = {α-Acyl lactams in the synthesis of physiologically active compounds},
journal = {Russian Chemical Reviews},
year = {2009},
volume = {78},
publisher = {ANO Editorial Board of the journal Uspekhi Khimii},
month = {Nov},
url = {https://rcr.colab.ws/publications/10.1070/RC2009v078n05ABEH004045},
number = {5},
pages = {431--456},
doi = {10.1070/RC2009v078n05ABEH004045}
}
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Nenajdenko, Valentin Georgievich, et al. “α-Acyl lactams in the synthesis of physiologically active compounds.” Russian Chemical Reviews, vol. 78, no. 5, Nov. 2009, pp. 431-456. https://rcr.colab.ws/publications/10.1070/RC2009v078n05ABEH004045.
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Abstract

Data on the methods of synthesis and the reactivity of α-acyl lactams are described systematically and generalized. The attention is focused on the recent achievements in the synthesis of heterocyclic compounds and biologically active substances from α-acyl lactams and cyclic imines derived from the latter compounds.